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食管癌患者唾液糖蛋白的异常糖型

The Abnormal Glycopatterns of Salivary Glycoproteins in Esophageal Squamous Cell Carcinoma Patients.

作者信息

Shu Jian, Ma Jun, Ren Xiameng, Wang Jian, Wang Yan, Zhang Kun, Yu Hanjie, Guo Xiangqian, Li Zheng

机构信息

Laboratory for Functional Glycomics, College of Life Sciences, Northwest University, Xi'an, China.

Institute of Digestive Disease of Zhengzhou University, Zhengzhou, China.

出版信息

Front Chem. 2021 Mar 4;9:637730. doi: 10.3389/fchem.2021.637730. eCollection 2021.

Abstract

Glycosylation is one of the most crucial posttranslational modifications of proteins, containing a remarkable amount of biological information. The alteration of glycosylation is closely associated with certain diseases. Exploring glyco-code in the development of diseases is a hot topic in recent years. Esophageal squamous cell carcinoma (ESCC) is the primary pathological histology in developing countries and a severe threat to human health. Although the glycan profiles in the blood samples of ESCC patients were analyzed using glycomic and glycoproteomic methods, the difference of salivary glycopatterns between healthy subjects and ESCC patients is not explicit yet. In the present study, ESCC patients (n = 16) and healthy volunteers (HVs, n = 25) were enrolled. The glycomic strategy combining lectin microarray and lectin blotting was employed to investigate and confirm the altered salivary glycopatterns. Datura stramonium (DSA) was selected to isolate the GlcNAc or Galβ1-4GlcNA-containing glycoproteins due to the distinct difference between ESCC patients and HVs. The N-glycans from DSA-enriched glycoproteins were released by PNGase F and further identified by MALDI-TOF/TOF-MS to obtain the precise structural information of the altered glycans. As a result, the glycopatterns recognized by 13 lectins (e.g., ECA, RCA120, and DSA) showed significant alterations in ESCC patients' saliva. The ESCC patients showed higher levels of GalNAc and Gal, sialic acid, and GlcNAc expression profiles and lower levels of mannose and fucose expression profiles. The MALDI-TOF/TOF-MS results indicated that the proportion of the GlcNAc or Galβ1-4GlcNAc-containing N-glycans was increased in ESCC patients (79.04%) compared with HV (63.20%), which was consistent with the results of lectin microarrays. Our findings provide comprehensive information to understand the complex physiological changes in ESCC patients. And the altered salivary glycopatterns such as GlcNAc or Galβ1-4GlcNAc-containing N-glycans recognized by DSA might serve as potential biomarkers for the diagnosis of ESCC patients.

摘要

糖基化是蛋白质最重要的翻译后修饰之一,蕴含着大量生物学信息。糖基化的改变与某些疾病密切相关。探索疾病发展过程中的糖密码是近年来的一个热门话题。食管鳞状细胞癌(ESCC)是发展中国家主要的病理组织学类型,对人类健康构成严重威胁。虽然已使用糖组学和糖蛋白质组学方法分析了ESCC患者血液样本中的聚糖谱,但健康受试者与ESCC患者唾液糖模式的差异尚不明确。在本研究中,纳入了ESCC患者(n = 16)和健康志愿者(HV,n = 25)。采用凝集素微阵列和凝集素印迹相结合的糖组学策略来研究和确认唾液糖模式的改变。由于ESCC患者与HV之间存在明显差异,选择曼陀罗(DSA)来分离含GlcNAc或Galβ1-4GlcNA的糖蛋白。通过PNGase F从DSA富集的糖蛋白中释放N-聚糖,并通过MALDI-TOF/TOF-MS进一步鉴定,以获得改变聚糖的精确结构信息。结果显示ESCC患者唾液中13种凝集素(如ECA、RCA120和DSA)识别的糖模式有显著改变。ESCC患者的GalNAc、Gal、唾液酸和GlcNAc表达谱水平较高,而甘露糖和岩藻糖表达谱水平较低。MALDI-TOF/TOF-MS结果表明,与HV(63.20%)相比,ESCC患者中含GlcNAc或Galβ1-4GlcNAc的N-聚糖比例增加(79.04%),这与凝集素微阵列的结果一致。我们的研究结果为理解ESCC患者复杂的生理变化提供了全面信息。并且,DSA识别的如含GlcNAc或Galβ1-4GlcNAc的N-聚糖等改变的唾液糖模式可能作为ESCC患者诊断的潜在生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fafa/7969727/67fa74fed08d/fchem-09-637730-g001.jpg

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